Model Number CD3357-40C |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problems
Death (1802); No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 10/20/2020 |
Event Type
Death
|
Manufacturer Narrative
|
Further information was requested but not provided.
|
|
Event Description
|
Related manufacturer reference number: 2017865-2021-09005.It was reported that the patient has deceased.There was no known allegation from a health care professional that suggests that the death was device related.The cause of death was cardiopulmonary arrest.No additional information was reported.
|
|
Manufacturer Narrative
|
The device was returned due to patient death.The device was tested on the bench [and using automated testing equipment,] and no anomalies were found.
|
|
Search Alerts/Recalls
|